“Emmy! Emmy!
Emmy! Emmy!” That is rapidly
becoming one of my very favorite things to hear, which is saying something
because I typically detest being called “Emmy”.
However when it’s coming out of the mouth of a 28 pound, 31 inch tall
blonde haired boy it’s an entirely different story. My nephew Jeremiah has me so tightly wrapped
around his finger (and I’m sure he knows it, he’s brilliant after all) that he
could call me practically anything and I’d love it. After the yelling of names and running
towards each other we end up hand to foot, his hands braced against the bottoms
of my feet. As he pulls my feet apart (I
say “he” because he tries, but really I do the heavy lifting) to clear room on
my chair to sit with me I pull him up sit on my lap. After I force him to give me a hug he settles
in on my lap between my braces and we’re off.
Jer has been sitting with me in my chair since the day he was born, and
I always thought that as he grew up into a little person he wouldn’t want to,
or he wouldn’t sit still as I turn the wheels.
However it’s just the opposite, it isn’t until I stop moving that he
gets antsy, most likely thinking that if he wiggles around enough the chair
will magically start to move again.
As one would anticipate the more
Jer develops the more he discovers about the world he lives in, thus making him
more curious about his aunt who’s different than everybody. I tend to be fairly oblivious to how people
perceive my chair, but I’m trying to be more conscious about that – partly
because it’s just plain interesting to know what others think of you and why
they think it. The first time I remember
my disability causing Jer to think is when he was sitting on my lap while I had
my braces on. I wear full length (foot to
upper thigh) braces with lockable knee joints.
My braces are like weirdly shaped metal legs – not super comfy to lean
against. One day Jer climbed up on my
lap, settled in his usual place and suddenly got this very disgusted look on
his face. He hit my brace, squawked
something in baby gibberish that I’m sure meant, “Dude Auntie Em what’s with
the hard legs?!?”, and then he grabbed the end of my pant leg and tried to
inspect what was making my lap feel different.
The tailoring of my pants didn’t allow him to inspect my braces much
though, which frustrated him for about half of a millisecond and then life
moved on.
A few days later we were at my
house and I went into my room to grab something. As I’ve come to expect Jer followed after me
to inspect everything he could get his hands on. There on my floor laid my braces and I saw a
teachable moment. I encouraged him to
manipulate them, pull the Velcro straps, slide the knee locks, knock on the
hard fiberglass backs. After he was done
inspecting them I put one on over my non-braced, pajama clad leg so he could
see. He stared with wide eyes as he
watched my normal legs put a different costume on. Once braced I pulled him up on my lap like we
normally would so he could see what he feels when he sits on my lap.
Knowing that the chances of him
remembering all the discoveries he made that afternoon were slim I still felt
it important to encourage him to make those connections. I’ve never had the opportunity to be the sole
person that someone bases their opinion about people in wheelchairs on. Spending so much time with Jer has really
spurred me to be cognizant of how the perceptions of people are crafted. My hope is that he grows up with a healthy
curiosity about not only what makes people different, but about his entire
world. I want him to not only wonder and
question, but be mindful enough to try and understand that which he doesn’t
know. What a different place the world
would be if as much as people questioned, they allowed themselves to learn and
be taught with an attitude of understanding and not simply knowing.
This is terrific! You write so well! I can "see" the story! Thank you!
ReplyDelete